Immunosenescence and multiple sclerosis: inflammaging for prognosis and therapeutic consideration.

IF 3.3 Q2 GERIATRICS & GERONTOLOGY
Frontiers in aging Pub Date : 2023-10-13 eCollection Date: 2023-01-01 DOI:10.3389/fragi.2023.1234572
Smathorn Thakolwiboon, Elizabeth A Mills, Jennifer Yang, Jonathan Doty, Martin I Belkin, Thomas Cho, Charles Schultz, Yang Mao-Draayer
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引用次数: 0

Abstract

Aging is associated with a progressive decline of innate and adaptive immune responses, called immunosenescence. This phenomenon links to different multiple sclerosis (MS) disease courses among different age groups. While clinical relapse and active demyelination are mainly related to the altered adaptive immunity, including invasion of T- and B-lymphocytes, impairment of innate immune cell (e.g., microglia, astrocyte) function is the main contributor to disability progression and neurodegeneration. Most patients with MS manifest the relapsing-remitting phenotype at a younger age, while progressive phenotypes are mainly seen in older patients. Current disease-modifying therapies (DMTs) primarily targeting adaptive immunity are less efficacious in older patients, suggesting that immunosenescence plays a role in treatment response. This review summarizes the recent immune mechanistic studies regarding immunosenescence in patients with MS and discusses the clinical implications of these findings.

Abstract Image

免疫衰老和多发性硬化症:炎症对预后和治疗的影响。
衰老与先天和适应性免疫反应的逐渐下降有关,称为免疫衰老。这种现象与不同年龄组的不同多发性硬化症(MS)病程有关。虽然临床复发和活动性脱髓鞘主要与适应性免疫的改变有关,包括T和B淋巴细胞的侵袭,但先天免疫细胞(如小胶质细胞、星形胶质细胞)功能的损伤是导致残疾进展和神经退行性变的主要原因。大多数多发性硬化症患者在较年轻时表现出复发-缓解表型,而进行性表型主要见于老年患者。目前主要针对适应性免疫的疾病改良疗法(DMTs)在老年患者中效果较差,这表明免疫衰老在治疗反应中发挥作用。这篇综述总结了最近关于多发性硬化症患者免疫衰老的免疫机制研究,并讨论了这些发现的临床意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
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审稿时长
13 weeks
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